QUALITY ASSURANCE

Quality Assurance at Surge means totality of arrangement for quality drugs which includes cGMP Compliance Monitoring at Production, Quality Control, Utilities, Material Management, Administration & Regulatory Compliance which has direct & indirect impact on product Quality, Safety, Purity & Efficacy.

Quality Assurance at Surge is independent & committed to ensure that the entire operations of its manufacturing facility meets the required cGMP standards and products manufactured therein conforms to the internationally accepted standards throughout its shelf life.

Execution of Validation Master Plan through Annual Validation Plan & we at Surge Labs is successively complying the validation requirement like.,
Utilities/System Qualification (HVAC, Water, Compressed Air, Pure Steam)
Equipment Qualification
Analytical Method Validation
Process Validation
Aseptic Process Validation
Cleaning Validation
Computer System Validation
Supplier Qualification with coordination of Supply Chain Management is base of quality raw materials & packaging components. QA has emphasis upon Analysis of Data through Annual Product Review (APR), Quality Risk Management (QRM), Handling & Investigation of Compliant, Deviation & Change Control, Self Inspection/Technical Audit & cGMP Training Plan to Worker & Executive Staff. QA has microscopic role at Surge & everything has to pass through it.